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Clinical Comparative Study to Validate Performance of SafeSed Prototype Monitoring Endoscopy Under Sedation

NCT02968797 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2018-03-21

No results posted yet for this study

Summary

SafeSed prototype monitors respiratory parameters by tracking chest movements with optical and accelerometer markers. The respiratory parameters are compared to respiratory parameters measured by a spirometer and a capnograph.

Conditions

  • Apnea

Interventions

DEVICE

SafeSed

Monitor respiratory parameters

Sponsors & Collaborators

  • Meir Medical Center

    lead OTHER

Principal Investigators

  • Brian Fredman, MD · Israel: Clalit Health bServices

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-01
Primary Completion
2019-12-01
Completion
2019-12-01

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02968797 on ClinicalTrials.gov